α-CoMoO4β-CoMoO4的制备及电化学性能研究

皇甫战彪1,2, 郭东方1,2, 梁黎明1,2, 刘雪坤1,2, 梁永福1,2, 程学瑞1,2, 杨坤1,2*

化工新型材料 ›› 2023, Vol. 51 ›› Issue (3) : 289 -293.

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化工新型材料 ›› 2023, Vol. 51 ›› Issue (3) : 289-293. DOI: 10.19817/j.cnki.issn1006-3536.2023.03.051
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α-CoMoO4β-CoMoO4的制备及电化学性能研究

    皇甫战彪1,2, 郭东方1,2, 梁黎明1,2, 刘雪坤1,2, 梁永福1,2, 程学瑞1,2, 杨坤1,2*
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Preparation and electrochemical properties of α-CoMoO4 and β-CoMoO4

  • Huangfu Zhanbiao1,2, Guo Dongfang1,2, Liang Liming1,2, Liu Xuekun1,2, Liang Yongfu1,2, Cheng Xuerui1,2, Yang Kun1,2
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摘要

采用水热法成功合成CoMoO4样品,采用X射线衍射、拉曼光谱和电学化学工作站研究了退火温度对样品结构和电化学性能的影响。结果表明,低温制备样品为β相CoMoO4,高于600℃退火时向高温相α-CoMoO4转变,1000℃时完全相变为高温α-CoMoO4。伴随βα相变,其在可见光区域的吸收增强,且光学带隙逐渐减小。电化学研究结果表明,两种结构的CoMoO4都具有典型的赝电容特性,但α-CoMoO4具有更低的瓦尔堡阻抗,且充放电容量明显大于β-CoMoO4,证实α-CoMoO4具有更优越的电容性能,在储能领域存在较大的应用前景。

Abstract

In the present work,CoMoO4 samples were successfully synthesized by hydrothermal method.The effects of annealing temperature on the structures and electrochemical properties of the samples were investigated by X-ray diffraction,Raman spectroscopy and electrochemical workstation.The results showed that the β phase CoMoO4 sample was obtained at low temperature.It transformed to α-CoMoO4 when the annealing temperature was above 600℃,and the β→α phase transition was finally completed at 1000℃.Along with the β→α phase transition,its absorption was obviously enhanced in the visible region and its optical band gap was gradually reduced.The electrochemical result exhibited that both CoMoO4 samples of two structures had typical pseudocapacitance characteristics.However,α-CoMoO4 had much lower Valborg resistance and significantly larger charge/discharge capacity than β-CoMoO4.Consequently,it was confirmed that α-CoMoO4 had superior capacitance performance to β-CoMoO4 and had great application prospects in the field of energy storage.

关键词

水热法 / CoMoO4 / 电化学 / 超级电容器 / 吸收光谱

Key words

hydrothermal method / CoMoO4 / electrochemistry / supercapacitor / absorption spectroscopy

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α-CoMoO4β-CoMoO4的制备及电化学性能研究[J]. 化工新型材料, 2023, 51(3): 289-293 DOI:10.19817/j.cnki.issn1006-3536.2023.03.051

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基金资助

国家自然科学基金(12104415);河南省科技攻关项目(222102230012)

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